| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:70404171-70404373 | Common:3; Rare:42 | ||||
| chr8:70607636-70607868 | Common:4; Rare:70 | ||||
| chr8:70608213-70608528 | Common:3; Rare:92 | ||||
| chr8:70668968-70669370 | Common:2; Rare:156 | ||||
| chr8:71361739-71361842 | Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:73008638-73008916 | Common:1; Rare:98 | ||||
| chr8:73293150-73293369 | Common:2; Rare:61 | ||||
| chr8:73293941-73294263 | Common:2; Rare:98 | ||||
| chr8:73294421-73294608 | Common:1; Rare:72 | ||||
| chr8:73746789-73747115 | Common:4; Rare:93 | ||||
| chr8:73878818-73879088 | Common:5; Rare:137 | ||||
| chr8:73971893-73971990 | Rare:38 | ||||
| chr8:73972055-73972606 | Common:2; Rare:152 | ||||
| chr8:73976029-73976337 | Common:6; Rare:110; Clinvar:3; Clinvar (benign):4 | ||||
| chr8:74350261-74350468 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):2 |